WormBase Tree Display for DO_term: DOID:0111022

DOID:0111022 Name: cone-rod dystrophy 16
  Status: Valid
  Definition: A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22.
  Synonym: Exact: CORD16
      retinal dystrophy with early macular involvement
  Parent: Is_a: DOID:0050572
  DB_info: Database: OMIM disease 614500